NDC Code | 72476-192-04 |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-04) > 30 TABLET in 1 BOTTLE, PLASTIC |
Product NDC | 72476-192 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Allergy Relief |
Non-Proprietary Name | Fexofenadine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20210714 |
Marketing Category Name | ANDA |
Application Number | ANDA211075 |
Manufacturer | RETAIL BUSINESS SERVICES , LLC. |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength | 180 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |